Sustained changes in digestive physiology and microbiome across sequential generations of zebrafish fed different diets
Alterations to ratios of protein and fiber in an organism's diet have been shown to structurally and functionally alter its individual digestive physiology. However, it is unclear how these dietary changes may affect phenotypic changes across generations. We utilized feeding trials, morphologic...
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Veröffentlicht in: | Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 2022-11, Vol.273, p.111285-111285, Article 111285 |
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creator | Leigh, Samantha C. Catabay, Caitlyn German, Donovan P. |
description | Alterations to ratios of protein and fiber in an organism's diet have been shown to structurally and functionally alter its individual digestive physiology. However, it is unclear how these dietary changes may affect phenotypic changes across generations. We utilized feeding trials, morphological analyses, enzyme activities, and 16S rRNA sequencing of the gut microbiome of zebrafish (Danio rerio) to determine how variations to fiber and protein concentrations, kept consistent across sequential generations, affect phenotypic changes. Our results show that Parental (P) and first generation (F1) fish did not differ from each other in terms of their intestine length, intestine mass, enzyme activity levels, and microbial community composition for any of the three experimental diets (high-protein/low-fiber, moderate-protein/fiber, and low-protein/high-fiber). However, each of the three experimental diets for the P and F1 fish, as well as the ancestral diet fish, did have distinct microbial community structure from one another. This indicates that there is a strong dietary effect on digestive physiology and gut microbial community and that these effects are consistent when the diet is kept homogenous across generations.
•Effects of diet on gut structure and function persist among generations.•Microbiome changes were also consistent with diet.•Overall microbiome changes still constrained by starting community.•Largest microbiome changes were the abundance of species already present.•Some rare species' abundance increased with diet treatments. |
doi_str_mv | 10.1016/j.cbpa.2022.111285 |
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•Effects of diet on gut structure and function persist among generations.•Microbiome changes were also consistent with diet.•Overall microbiome changes still constrained by starting community.•Largest microbiome changes were the abundance of species already present.•Some rare species' abundance increased with diet treatments.</description><identifier>ISSN: 1095-6433</identifier><identifier>EISSN: 1531-4332</identifier><identifier>DOI: 10.1016/j.cbpa.2022.111285</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>16S rRNA ; community structure ; Danio rerio ; Digestive enzymes ; digestive physiology ; enzyme activity ; enzymes ; fish ; intestinal microorganisms ; intestines ; Microbes ; microbial communities ; microbiome ; Morphology ; phenotype ; Phenotypic changes</subject><ispartof>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 2022-11, Vol.273, p.111285-111285, Article 111285</ispartof><rights>2022 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-1ddf6ccd803a53c09aec1f592cba0e40faee4d5df79cf7cc9a0bbfcaa776a8143</citedby><cites>FETCH-LOGICAL-c410t-1ddf6ccd803a53c09aec1f592cba0e40faee4d5df79cf7cc9a0bbfcaa776a8143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S109564332200143X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Leigh, Samantha C.</creatorcontrib><creatorcontrib>Catabay, Caitlyn</creatorcontrib><creatorcontrib>German, Donovan P.</creatorcontrib><title>Sustained changes in digestive physiology and microbiome across sequential generations of zebrafish fed different diets</title><title>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</title><description>Alterations to ratios of protein and fiber in an organism's diet have been shown to structurally and functionally alter its individual digestive physiology. However, it is unclear how these dietary changes may affect phenotypic changes across generations. We utilized feeding trials, morphological analyses, enzyme activities, and 16S rRNA sequencing of the gut microbiome of zebrafish (Danio rerio) to determine how variations to fiber and protein concentrations, kept consistent across sequential generations, affect phenotypic changes. Our results show that Parental (P) and first generation (F1) fish did not differ from each other in terms of their intestine length, intestine mass, enzyme activity levels, and microbial community composition for any of the three experimental diets (high-protein/low-fiber, moderate-protein/fiber, and low-protein/high-fiber). However, each of the three experimental diets for the P and F1 fish, as well as the ancestral diet fish, did have distinct microbial community structure from one another. This indicates that there is a strong dietary effect on digestive physiology and gut microbial community and that these effects are consistent when the diet is kept homogenous across generations.
•Effects of diet on gut structure and function persist among generations.•Microbiome changes were also consistent with diet.•Overall microbiome changes still constrained by starting community.•Largest microbiome changes were the abundance of species already present.•Some rare species' abundance increased with diet treatments.</description><subject>16S rRNA</subject><subject>community structure</subject><subject>Danio rerio</subject><subject>Digestive enzymes</subject><subject>digestive physiology</subject><subject>enzyme activity</subject><subject>enzymes</subject><subject>fish</subject><subject>intestinal microorganisms</subject><subject>intestines</subject><subject>Microbes</subject><subject>microbial communities</subject><subject>microbiome</subject><subject>Morphology</subject><subject>phenotype</subject><subject>Phenotypic changes</subject><issn>1095-6433</issn><issn>1531-4332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFUU1PGzEQtaoiAWn_ACcfe9nU493NZqVeECoUCYkD9GzNjseJo40d7A1V-PV1Gs50LvNGem--nhBXoOagYPF9M6dhh3OttJ4DgF62n8QFtDVUTV3rzwWrvq0WpTgXlzlvVIkGmgvx52mfJ_SBraQ1hhVn6YO0voDJv7LcrQ_ZxzGuDhKDlVtPKQ4-blliQTnLzC97DpPHUa44cMLJx5BldPKNh4TO57V0pbv1znEqzIJ4yl_EmcMx89f3PBO_b38-3_yqHh7v7m-uHypqQE0VWOsWRHapamxrUj0ygWt7TQMqbpRD5sa21nU9uY6oRzUMjhC7boFLaOqZ-Hbqu0uxLJons_WZeBwxcNxnoztY1i00ZcD_qUpD17fliTOhT9R_P0jszC75LaaDAWWOhpiNORpijoaYkyFF9OMk4nLvq-dkMnkOxNYnpsnY6D-S_wVJkpf0</recordid><startdate>202211</startdate><enddate>202211</enddate><creator>Leigh, Samantha C.</creator><creator>Catabay, Caitlyn</creator><creator>German, Donovan P.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202211</creationdate><title>Sustained changes in digestive physiology and microbiome across sequential generations of zebrafish fed different diets</title><author>Leigh, Samantha C. ; Catabay, Caitlyn ; German, Donovan P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-1ddf6ccd803a53c09aec1f592cba0e40faee4d5df79cf7cc9a0bbfcaa776a8143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>16S rRNA</topic><topic>community structure</topic><topic>Danio rerio</topic><topic>Digestive enzymes</topic><topic>digestive physiology</topic><topic>enzyme activity</topic><topic>enzymes</topic><topic>fish</topic><topic>intestinal microorganisms</topic><topic>intestines</topic><topic>Microbes</topic><topic>microbial communities</topic><topic>microbiome</topic><topic>Morphology</topic><topic>phenotype</topic><topic>Phenotypic changes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leigh, Samantha C.</creatorcontrib><creatorcontrib>Catabay, Caitlyn</creatorcontrib><creatorcontrib>German, Donovan P.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leigh, Samantha C.</au><au>Catabay, Caitlyn</au><au>German, Donovan P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sustained changes in digestive physiology and microbiome across sequential generations of zebrafish fed different diets</atitle><jtitle>Comparative biochemistry and physiology. Part A, Molecular & integrative physiology</jtitle><date>2022-11</date><risdate>2022</risdate><volume>273</volume><spage>111285</spage><epage>111285</epage><pages>111285-111285</pages><artnum>111285</artnum><issn>1095-6433</issn><eissn>1531-4332</eissn><abstract>Alterations to ratios of protein and fiber in an organism's diet have been shown to structurally and functionally alter its individual digestive physiology. However, it is unclear how these dietary changes may affect phenotypic changes across generations. We utilized feeding trials, morphological analyses, enzyme activities, and 16S rRNA sequencing of the gut microbiome of zebrafish (Danio rerio) to determine how variations to fiber and protein concentrations, kept consistent across sequential generations, affect phenotypic changes. Our results show that Parental (P) and first generation (F1) fish did not differ from each other in terms of their intestine length, intestine mass, enzyme activity levels, and microbial community composition for any of the three experimental diets (high-protein/low-fiber, moderate-protein/fiber, and low-protein/high-fiber). However, each of the three experimental diets for the P and F1 fish, as well as the ancestral diet fish, did have distinct microbial community structure from one another. This indicates that there is a strong dietary effect on digestive physiology and gut microbial community and that these effects are consistent when the diet is kept homogenous across generations.
•Effects of diet on gut structure and function persist among generations.•Microbiome changes were also consistent with diet.•Overall microbiome changes still constrained by starting community.•Largest microbiome changes were the abundance of species already present.•Some rare species' abundance increased with diet treatments.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.cbpa.2022.111285</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 16S rRNA community structure Danio rerio Digestive enzymes digestive physiology enzyme activity enzymes fish intestinal microorganisms intestines Microbes microbial communities microbiome Morphology phenotype Phenotypic changes |
title | Sustained changes in digestive physiology and microbiome across sequential generations of zebrafish fed different diets |
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